A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724192



Internal ID147858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52599659..52946366hg38UCSC Ensembl
chr19:53102912..53449619hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38346708
hg19346708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531059
Supporting Variants
Samples
Known GenesZNF137P, ZNF28, ZNF320, ZNF321P, ZNF468, ZNF600, ZNF611, ZNF816-ZNF321P, ZNF83
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724192
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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